Biomet, Inc. · Class II · Cleared Jul 3, 2014
| K-number | K140902 |
| Device name | E1 SERIES A PATELLAE, STANDARD 3-PEG, E1 SERIES A PATELLAE, THIN 3-PEG, E1 SERIES PATELLAE, ASYMMETRICAL, 3-PEG |
| Applicant | Biomet, Inc. |
| Product code | JWH |
| Device class | Class II |
| Decision date | Jul 3, 2014 |
| Decision | Substantially Equivalent |
| Regulation | 888.3560 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov